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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 11, 2000
The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation
A F Struyk, K A Scoggan, D E Bulman, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1990
Genetic and biochemical determinations in the pre-transplant workup and in the post-transplant assessment period
R G Worton, D E Bulman, E E Zubrzycka-Gaarn, et al.
Neurology
|
July 23, 2003
Mutations in the epsilon-sarcoglycan gene found to be uncommon in seven myoclonus-dystonia families
F Han, A E Lang, L Racacho, et al.
Journal of Medical Genetics
|
May 24, 2001
Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2
K A Scoggan, T Chandra, R Nelson, et al.
Archives of Neurology
|
June 1, 1991
The influence of gender on the susceptibility to multiple sclerosis in sibships
A D Sadovnick, D E Bulman, L Hashimoto, et al.
Epilepsia
|
February 26, 2000
Evidence favoring genetic heterogeneity for febrile convulsions
L J Racacho, R S McLachlan, G C Ebers, et al.
Neurology
|
September 1, 1992
Premature chain termination mutation causing Duchenne muscular dystrophy
P R Clemens, P A Ward, C T Caskey, et al.
Annals of Neurology
|
October 1, 1986
Absence of antibody to HTLV I and III in sera of Canadian patients with multiple sclerosis and chronic myelopathy
G P Rice, H A Armstrong, D E Bulman, et al.
Human Molecular Genetics
|
February 1, 1995
Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p
B von Brederlow, A F Hahn, W J Koopman, et al.
American Journal of Human Genetics
|
June 1, 1989
Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy gene
X Y Hu, A H Burghes, D E Bulman, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 52) with videos related to
Sort By:
Page
of 6
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 11, 2000
The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation
A F Struyk, K A Scoggan, D E Bulman, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1990
Genetic and biochemical determinations in the pre-transplant workup and in the post-transplant assessment period
R G Worton, D E Bulman, E E Zubrzycka-Gaarn, et al.
Neurology
|
July 23, 2003
Mutations in the epsilon-sarcoglycan gene found to be uncommon in seven myoclonus-dystonia families
F Han, A E Lang, L Racacho, et al.
Journal of Medical Genetics
|
May 24, 2001
Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2
K A Scoggan, T Chandra, R Nelson, et al.
Archives of Neurology
|
June 1, 1991
The influence of gender on the susceptibility to multiple sclerosis in sibships
A D Sadovnick, D E Bulman, L Hashimoto, et al.
Epilepsia
|
February 26, 2000
Evidence favoring genetic heterogeneity for febrile convulsions
L J Racacho, R S McLachlan, G C Ebers, et al.
Neurology
|
September 1, 1992
Premature chain termination mutation causing Duchenne muscular dystrophy
P R Clemens, P A Ward, C T Caskey, et al.
Annals of Neurology
|
October 1, 1986
Absence of antibody to HTLV I and III in sera of Canadian patients with multiple sclerosis and chronic myelopathy
G P Rice, H A Armstrong, D E Bulman, et al.
Human Molecular Genetics
|
February 1, 1995
Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p
B von Brederlow, A F Hahn, W J Koopman, et al.
American Journal of Human Genetics
|
June 1, 1989
Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy gene
X Y Hu, A H Burghes, D E Bulman, et al.
Page
of 6